A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891006



Internal ID18838716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:60392..176270hg38UCSC Ensembl
Outerchr7:40922..223067hg38UCSC Ensembl
Innerchr7:60392..176270hg19UCSC Ensembl
Outerchr7:40922..223067hg19UCSC Ensembl
Innerchr7:155475..271353hg18UCSC Ensembl
Outerchr7:136005..318150hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38182146
hg19182146
hg18182146
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789200, essv25788512
Samples
Known GenesFAM20C, LOC100507642
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891006
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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